Clinical trials
Full profile accessFollow clinical development from trial design and recruitment through results.
- Trial phase
- Status
- Readouts
Company intelligence / Profile preview
Fareva SIMS is a specialized contract development and manufacturing organization (CDMO) that focuses on the production of high-potency active pharmaceutical ingredients (HPAPIs). Located in Saint-Quentin-Fallavier, France, the facility is recognized as a center of excellence for the chemical synthesis of steroids and hormonal substances. Originally established as a manufacturing site for Pfizer (formerly Upjohn), it was acquired by the Fareva Group in 2004 to enhance its global chemical production capabilities. The company provides a range of services from process optimization and pilot-scale development to full-scale industrial manufacturing under strict Good Manufacturing Practice (GMP) standards. Fareva SIMS serves major pharmaceutical clients globally, supporting the supply chain for treatments in endocrinology and inflammatory diseases.
Beyond the preview
Explore clinical development, deal activity, and the competitive landscape with Gosset’s full data platform.
Follow clinical development from trial design and recruitment through results.
Explore licensing agreements, acquisitions, and the assets behind each deal.
Trace financing activity and the investors behind a company’s development.
Compare peer pipelines by target, modality, and therapeutic area.
Explore technology platforms and the patent landscape around relevant assets.
Connect company news and source material to the questions you’re investigating.
See how Gosset can support your research on Fareva SIMS.